Martens Joseph A, Wu Pei-Yun Jenny, Winston Fred
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2005 Nov 15;19(22):2695-704. doi: 10.1101/gad.1367605.
Recent studies have revealed that transcription of noncoding, intergenic DNA is abundant among eukaryotes. However, the functions of this transcription are poorly understood. We have previously shown that in Saccharomyces cerevisiae, expression of an intergenic transcript, SRG1, represses the transcription of the adjacent gene, SER3, by transcription interference. We now show that SRG1 transcription is regulated by serine, thereby conferring regulation of SER3, a serine biosynthetic gene. This regulation requires Cha4, a serine-dependent activator that binds to the SRG1 promoter and is required for SRG1 induction in the presence of serine. Furthermore, two coactivator complexes, SAGA and Swi/Snf, are also directly required for activation of SRG1 and transcription interference of SER3. Taken together, our results elucidate a physiological role for intergenic transcription in the regulation of SER3. Moreover, our results demonstrate a mechanism by which intergenic transcription allows activators to act indirectly as repressors.
最近的研究表明,非编码基因间DNA的转录在真核生物中很普遍。然而,这种转录的功能却鲜为人知。我们之前已经表明,在酿酒酵母中,基因间转录本SRG1的表达通过转录干扰抑制相邻基因SER3的转录。我们现在发现,SRG1的转录受丝氨酸调控,从而实现对丝氨酸生物合成基因SER3的调控。这种调控需要Cha4,一种丝氨酸依赖性激活因子,它与SRG1启动子结合,并且在有丝氨酸存在时是SRG1诱导所必需的。此外,两种共激活因子复合物SAGA和Swi/Snf,也是SRG1激活和SER3转录干扰直接所需的。综上所述,我们的结果阐明了基因间转录在SER3调控中的生理作用。此外,我们的结果还证明了一种机制,通过该机制基因间转录使激活因子能够间接作为抑制因子发挥作用。